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Overlap syndromes are diseases that meet the criteria of two or more rheumatic diseases. In this case report, a woman in her 20s presented with a constellation of symptoms, including skin thickening, Raynaud's phenomenon, hypertension, absent pulse in both lower limbs with bilateral renal artery bruit. The antinuclear antibody profile revealed Scl-70 positivity. CT thorax identified early interstitial lung disease, and nailfold capillaroscopy showed severe capillary loss. CT angiogram features were suggestive of Takayasu arteritis. Notably, there have been only four documented cases of systemic sclerosis coexisting with Takayasu arteritis, highlighting the rarity of this overlap syndrome. The diagnosis of overlap syndrome was made after a thorough history recording and clinical examination. In the presence of bilateral renal artery stenosis, managing the scleroderma renal crisis may be challenging . This patient received treatment with mycophenolate mofetil and oral corticosteroids, aiming to address both systemic sclerosis and Takayasu arteritis effectively.
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http://dx.doi.org/10.1136/bcr-2023-256858 | DOI Listing |
Rev Clin Esp (Barc)
September 2025
Servicio de Medicina Interna, Unidad de Ecografía Clínica, Hospital San Carlos, San Fernando, Cádiz, Spain. Electronic address:
BMJ Case Rep
September 2025
Department of Nephrology, Christian Medical College, Vellore, Tamil Nadu, India
Renal involvement in Takayasu arteritis (TA) has been reported, but glomerular lesions causing nephrotic syndrome (NS) are rare. This is a case report of TA presenting with NS due to secondary amyloidosis.A woman in her late 40s was diagnosed as TA at the age of 15 years presented with nephrotic range proteinuria.
View Article and Find Full Text PDFJACC Case Rep
August 2025
Department of Radiology, Hospital México, San José, Costa Rica.
Case Summary: A 20-year-old woman presented with acute coronary syndrome. Invasive coronary angiography revealed complete occlusion of the left main coronary artery. Subsequent computed tomography angiography demonstrated occlusion of the left subclavian, left vertebral, and superior mesenteric arteries, along with circumferential thickening of the abdominal aorta, consistent with Takayasu arteritis.
View Article and Find Full Text PDFJACC Case Rep
August 2025
Paediatric Cardiothoracic Department, Alder Hey Children's Hospital, Liverpool, United Kingdom. Electronic address:
Background: Takayasu arteritis (TA) is a large-vessel vasculitis that primarily affects the aorta and the pulmonary and coronary arteries.
Case Summary: A 4-year-old boy was diagnosed in 2022 with pyoderma gangrenosum (PG) and required prolonged multidisciplinary care, including aggressive medical immunosuppression for severe skin lesions. In October 2024, after a period of clinical stability, he presented with a seizure and right-sided weakness.
Autoimmun Rev
August 2025
Departments of Medicine and Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Canada; Population Health Research Institute, Hamilton Health Sciences / McMaster University, Hamilton, Canada. Electronic address:
The fragility of randomized controlled trials (RCTs) of large vessel vasculitis (LVV) - defined as the minimum number of outcome events that would need to change to reverse the trial's conclusions - has not been comprehensively studied. We identified relevant RCTs with a systematic literature review till April 2025. The fragility index (FI)/ reverse fragility index (RFI) and fragility quotient (FQ, i.
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